Results 51 to 60 of about 4,755 (272)

PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia: a case-control study in southwest China

open access: yesJournal of Applied Oral Science, 2013
Our research aimed to look into the clinical traits and genetic mutations in sporadic non-syndromic anodontia and to gain insight into the role of mutations of PAX9, MSX1, AXIN2 and EDA in anodontia phenotypes, especially for the PAX9.
Jing WANG   +12 more
doaj   +1 more source

Prosthetic rehabilitation of siblings with oligodontia and metal allergy

open access: yesFogorvosi Szemle, 2022
Oligodontia is a complex congenital deformity, as it includes the lack of permanent teeth, functional and psychosocial problems. The management of this deformity requires a multidisciplinary approach, that involves the work of an orthodontist ...
Kata Kelemen   +2 more
doaj   +1 more source

Hypohidrotic ectodermal dysplasia with anodontia: A rare case-rehabilitation by prosthetic management

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2012
Ectodermal dysplasia is a hereditary disorder characterized by developmental dystrophies of ectodermal derivatives- It is characterized by triad of signs comprising sparse hair, abnormal or missing teeth and inability to sweat.
M Naveen Kumar   +5 more
doaj   +1 more source

Non-Syndrome Case of Multiple Erupted Supernumerary Teeth and Wisdom Tooth Anodontia

open access: yes, 2021
Supernumerary teeth can be detected during a routine clinical or radiographic examination. They are defined as any tooth or tooth substances that are excess of the usual configuration of twenty deciduous and thirty-two permanent teeth.
Nawaf Alzaben   +2 more
semanticscholar   +1 more source

Hereditary Hypohidrotic Ectodermal Dysplasia: Report of a Rare Case [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2013
Hereditary Hypohidrotic Ectodermal Dysplasia (HHED), an X-linked, recessive, Mendelian character, is seen usually in males and it is inherited through female carriers.
Geetha Paramkusam   +3 more
doaj   +1 more source

The association between Ponticulus Posticus and Dental Agenesis: a retrospective study [PDF]

open access: yes, 2018
OBJECTIVE: Neural tube defects may increase the risk of an abnormal development of skull, vertebral column and teeth formation, including dental agenesis in non syndromic patients. The association between the presence of a congenital Dental Agenesis (DA)
Barbato, Ersilia   +3 more
core   +1 more source

NUMERIC DENTAL ANOMALIES IN CHILDREN FROM CLUJ-NAPOCA [PDF]

open access: yesRomanian Journal of Stomatology, 2018
Numeric tooth anomalies involving a fewer number of teeth (hypodontia) are considered dental dystrophies determined by disturbances during the odontogenesis stage.
Viorica Ţărmure   +8 more
doaj   +1 more source

Prevalence of Talon cusp in Indian population [PDF]

open access: yes, 2012
Aim: To investigate the prevalence of the talon cusps in a sample of Indian dental patients and their distribution among different types of teeth. To determine the presence of other dental anomalies associated with the talon cusps.
Chatra, Laxmikanth   +5 more
core   +1 more source

Primary Teeth Supported Fixed Prosthesis—A Predictable Treatment Alternative

open access: yesChildren, 2022
Background: Individuals with tooth agenesis often present a significant clinical challenge for dental practitioners. This retrospective study evaluated clinical and radiological long-term functional and esthetic outcomes following restoration using ...
Sarit Naishlos   +8 more
doaj   +1 more source

Sanjad-Sakati Syndrome Dental Management: A Case Report [PDF]

open access: yes, 2013
Sanjad-Sakati syndrome (SSS) is a rare genetic disorder with autosomal recessive pattern of inheritance characterized by hypoparathyroidism, sever growth failure, mental retardation, susceptibility to chest infection, and dentofacial anomalies.
Hisham Y. El Batawi
core   +1 more source

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